BIOL-UA 21 Lecture Notes - Lecture 15: Oculopharyngeal Muscular Dystrophy, Restriction Fragment Length Polymorphism, Archibald Garrod

17 views4 pages
18 Mar 2016
Department
Professor

Document Summary

Molecular genetic analysis ii: cloning a human genome autosomal = not sex linked dominant = one bad copy of gene recessive = two copies of bad gene. Inheritance patterns of mendelian diseases: autosomal dominant, huntington"s disease: i. Ahd/a+ x a+/a+ (heterozygous) progeny will have 50% chance of contracting huntington"s: autosomal recessive, cystic fibrosis i. ii. Acftr/a+ x acftr/a+ both are carries progeny has 25% chance of contracting disease. Equal probability for sons and daughters: x-linked recessive, duchenne muscular dystrophy i. X+/y x xdmd/x+ probability for female progeny is 0%, probability of male to contract dmd is 50: mother had to be a carrier, and her mother had to be affected for a woman to receive sex-linked disease. Dominant inheritance predominantly in people of french canadian heritage and can be traced back to 3 french sisters who came to canada in 1648. The number of genetic diseases that are available for testing 4000.

Get access

Grade+
$40 USD/m
Billed monthly
Grade+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
10 Verified Answers
Class+
$30 USD/m
Billed monthly
Class+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
7 Verified Answers

Related Documents

Related Questions